Intravenous needle and Luer fitting securement

ABSTRACT

An IV holder for securing an IV needle and Luer fitting assembly. The IV holder includes a frame defining an aperture with a first portion and a second portion, the first portion of the aperture further being covered by a transparent window for protecting and securing the IV needle insertion site. The second portion of the aperture is disposed to fit a cylindrical Luer fitting. The holder is adhesively applied to a patient&#39;s skin and situated so that the needle insertion site is under the window and the first portion of the aperture while the Luer fitting is disposed within the second portion of the aperture.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of Ser. No. 11/316,076, filed on Dec.22, 2005, entitled, “METHOD AND APPARATUS FOR SECURING I.V. NEEDLE ANDLUER FITTING,” now U.S. Pat. No. 9,248,258, which claims priority fromU.S. Provisional Patent Application No. 60/662,419, filed on Mar. 16,2005, entitled, “METHOD AND APPARATUS FOR SECURING I.V. NEEDLE AND LUERFITTING,” the disclosures of which are hereby incorporated by referencein its entirety.

TECHNICAL FIELD OF THE INVENTION

The present invention relates generally to securement devices forstabilizing venous access devices such as intravenous needles and theirassociated Luer fittings to a patient's skin.

BACKGROUND OF THE INVENTION

intravenous (IV) needles are frequently used in medical procedures. Aswith any invasive procedure, IV-related infections are a significantconcern. Where repeated access to the bloodstream is needed, IVcatheters are used. These catheters frequently use cylindrical Luerfittings and valves as an alternative to traditional needle basedinjection ports. However, in order to be effective, catheters must avoiddislodgment as well as avoid bloodstream infection and local siteinfection.

IV catheter securement poses a number of challenges. In order tomaximize residence time, IV catheters must be secured from dislodgementor causing damage from unwanted movement. The insertion site should alsobe easily inspected for and protected from contamination or infection.Preferably, the catheter port can also be readily serviced.

Traditional methods call for securing the catheter insertion site with agauze dressing or a transparent film with adhesive tape. Adhesive tapeis problematic in that it is difficult to keep sterile and is prone toirritate a patient's skin. The use of a transparent film is preferablesince it serves as a pathogenic barrier and permits viewing of theinsertion site. However, transparent films are problematic in that thefilm eventually loosens from casual contact and permits cathetermigration.

The disparity in diameter between an IV needle and a Luer fittingfurther complicates the securement problem. While an adhesive strip canbe taped over the Luer fitting to secure the Luer fitting to the skin,the opaque tape prevents visual inspection of the Luer fitting.Moreover, securing the Luer fitting under a transparent film or underadhesive tape is problematic in that the larger diameter of the Luerfitting acts as a spacer and creates a gap between the film or tape andthe patient's skin. This gap defeats the infection barrier purpose ofsecurement.

Another approach is embodied by an IV holder produced by ConMed, Inc.,of Utica, N.Y., generally described in U.S. Pat. No. 4,669,458. TheConMed device is a catheter dressing with a generally tear-drop shapedframe with a base strip that completely encloses a polymer window. Inoperation, the polymer window is positioned over the area where theintravenous needle enters the skin and the body of a patient. Thetransparent cylindrical Luer fitting used to secure the intravenousneedle to a tubing assembly itself is adhesively secured taping down thebase strip over Luer fitting.

One significant disadvantage of the ConMed dressing is that because theLuer fitting is secured by and under the base strip, it is not readilyinspected for blockage. In addition, it is also difficult to disconnector replace the Luer fitting without removing the entire dressing. Yetanother disadvantage is that owing to the comparative larger diameter ofthe Luer fitting as compared to the intravenous needle and intravenoustubing, securing the Luer fitting with the dressing tends to create gapsbetween the elevated dressing and the patient's skin. This gap isdetrimental to a primary function of the IV holder, i.e., to seal thearea around the intravenous needle to prevent fluid and foreigncontaminants from entering the patient's body at the insertion site.

There is thus a need for a IV holder to alleviate the disadvantages ofthose IV holders available in the present art. Specifically, the IVholder of the present invention readily permits access to the Luerfitting and maintains a closer seal around the needle insertion site.

SUMMARY OF THE INVENTION

The present invention is related to IV holders. The holder comprises ofa frame made of a contoured or flexible material that is capable ofbeing secured to a patient's skin. The frame further defines an aperturewith a first portion and a second portion. A transparent window issecured to the first portion of the aperture while the second portion ofthe aperture is left open. The holder is used to secure an IV insertionsite by positioning the insertion site under the window in the firstportion of the aperture and the larger diameter Luer fitting in the opensecond portion of the aperture.

In a preferred embodiment, the holder is composed of a soft pliablematerial forming a frame. The frame surrounds an aperture with a firstportion and a second portion. A flexible transparent film is secured tothe frame over the first portion of the aperture to form a protectivebarrier over the first portion of the aperture. Preferably, at least aportion of the underside of the frame has an adhesive to facilitatesecurement of the IV holder on a patient's skin.

When placing the IV holder, the holder is positioned so that the filmcovered first portion of the aperture is over the IV needle insertionsite. The holder is further oriented so that the Luer fitting upstreamfrom the IV needle insertion site is placed in the second portion of theaperture.

The second portion of the frame is perforated for removal. This permitsaccess to and servicing of the Luer fitting without removing the holder.Additional adhesive strips are provided with the IV holder for securingthe Luer fitting or the IV apparatus upstream of the insertion site.These strips may also have a writable surface so that patientidentification or other information can be written thereon.

The components of the IV holder can also be made of more rigid materialsand contoured to fit around a patient's body by using a hard plastic fora frame and a clear plastic window with more rigidity. To ensure thebest possible fit, the outer surface of the Luer fitting can includeraised surfaces or depressions matching their complements on the Luerfitting to lock the cover onto the Luer fitting for additionalstability. The matching IV holder and Luer fitting can be provided inkit form.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 illustrates a preferred embodiment of the IV holder of theinvention;

FIG. 2 is a perspective view of the IV holder of FIG. 1;

FIG. 3 is an exploded view of the IV holder of FIG. 1;

FIG. 4 is a perspective view showing the IV holder of FIG. 1 inoperation with an IV needle, Luer fitting, and tubing;

FIG. 5 is an exploded view of an alternate embodiment of the IV holderof the present invention; and

FIG. 6 is an exploded view of a kit with an IV holder and anaccompanying Luer fitting.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

Referring now to the drawings, FIGS. 1-3 show a preferred embodiment ofthe IV holder of the present invention. The IV holder 10 includes frame15 and base strip 15A and further includes additional strips. The frame15 and base strip 15A define an aperture 20 with a first portion 30 anda second portion 35. The area of first portion 30 should be large enoughto surround an IV needle insertion site. While the first portion 30 ofthe aperture 20 is shown to be larger than the second portion 35, thisis not necessary so long as the second portion 35 is large enough toaccommodate the length of a Luer fitting.

While a horseshoe shape is depicted, frame 15 can be of any shape suchas circular, rectangular or other polygonal shapes. Curved shapes aremore preferred, however, because they are more resistant to dislodgingthe adhesive seal than hard edges and corners.

The bottom surface 21 of frame 15, base strip 15A, and strips 16 arecoated with an adhesive that facilitates the securement of the IV holder10 to the skin of a patient. The frame 15 is preferably made of a softpliable material with an adhesive back such as the 1/16 inchpolyethylene foam tape 1772 manufactured by 3M®. Additional strips 16may be fabricated from similar materials. It should also be understoodthat the frame 15 can be made of a more rigid material such as a hardplastic to resist removal and increase durability.

The adhesive underside of frame 15, base strip 15A, and strips 16 arereleasably secured to backing 45 until they are needed. A frangibleportion, such as a perforation 47, permit base strip 15A and itsadhesive backing to be detached from frame 15. Likewise, lines ofweakening or perforation 48 permit separation of strips 16 from frame 15and base strip 15A or from each other for separate application or toreservation for later use. Backing 45 can contain frangible portions topermit removal of the backing 45 from frame 15 by the operator with onehand.

The additional strips 16 provided can be used for a number of purposes.While the IV holder is initially secured by frame 15 and base strip 15A,base strip 15A is removable for servicing the Luer fitting. Whenservicing is complete, the Luer fitting can be resecured by using thestrip 16 in place of the removed base strip 15A. Strips 16 are also usedto secure the IV tubing upstream of the insertion site as shown in FIG.4. The surface of strip 16 may further include a writable surface forthe notation of patient identification or other information.

A window 40 covers the first portion 30 of the aperture 20. Theperipheral edge of the window 40 is permanently secured to frame 15.Window 40 preferably is made of a urethane or similar material and isflexible, clear, breathable and sterilizable to minimize contaminationwhen the IV holder is applied. The underside of window 40 optionallyincludes an adhesive coating to secure an IV needle (not shown) to theskin and minimize gaps between the window 40 and the skin to furtherminimize contamination. With these qualities, window 40 is positionedover and provides a viewable window to the insertion site so that anycontamination can be monitored while simultaneously providing a barrieraround the insertion site.

While not strictly necessary, there is a benefit to be obtained if theIV holder 10 is longer (i.e., in the Y direction) than it is wide (i.e.,in the X direction). A narrower width provides for better support andsecurement of the holder 10. Additionally, a longer length allows foradded versatility in the positioning of the holder relative to the Luerfitting.

FIG. 4 depicts the IV holder 10 in operation. Backing 45 is torn alonglines of weakening 48 to separate pieces 15 and 15A from pieces 16. AnIV needle 60 is inserted into the body of a patient at insertion site 65through the skin 67. The needle 60 is connected to Luer fitting 70, towhich the IV tubing 80 is connected. Backing 45 is removed from holderpieces 15 and 15A to expose the adhesive on the holder 10. The holder 10is then pressed against the skin 67 of the patient to cover the exposedportions of needle 60. Window 40 is positioned over the insertion site65 and is further positioned so that Luer fitting 70 is in the opensecond portion 35 of the aperture 20. In this position, insertion site65 can be visually inspected through the window 40 and the window 40 iscontoured around the needle 65 so as to be substantially in closeproximity or contact with the patient's skin 67.

The holder 10 is further preferably positioned so that cylindrical Luerfitting 70 is positioned in the second portion 35 of the aperture 20.This permits the Luer fitting to extend upwardly through the secondportion 35 of the aperture 20 and does not interfere with window 40.Base strip 15A is used to secure the IV tubing 80 to the patient's skinupstream of the Luer fitting 70. Further adhesive strips 16 are be usedto secure the IV tubing 80 at other positions to minimize the risk ofdislodging the IV assembly.

Secured in this manner, the window 40 of IV holder 10 provides a barrieragainst infection and contamination of and a way to visually inspect theinsertion site 65. Because the window 40 secures the IV needle 60, whichhas a small diameter in comparison to Luer fitting 70, the flexiblewindow 40 substantially contours around the diameter of the needle 60and establishes a seal by minimizing gaps between the window 40 and thepatient's skin 67. Luer fitting 70 is secured in part by base strip 15Aupstream and the holder 10 and window 40 downstream. By positioning theLuer fitting 70 in the second portion 35 of aperture 20, the excessiveheight and diameter of fitting 70 (in comparison to needle 60 and tubing80) does not interfere with the securement of the IV holder 10.

In the event that it is necessary to detach the Luer fitting 70 forservice or to clear needle 60, base strip 15A is readily removed bytearing along lines of weakening 47. Luer fitting 70 is then unthreadedfrom needle 60, serviced, and replaced without the need to remove orotherwise disturb frame 15 and window 40 of the IV holder 10. Once theservice is complete, the Luer fitting 70 and the IV tubing 80 is securedby one of the reserved adhesive strips 16.

FIG. 5 shows an shows an alternate preferred embodiment of the IV holder100 of the present invention. The IV holder comprises of a base frame101, a spacer frame 102, and a cover plate 103. Base frame 101 definesan aperture 110 and also includes a plurality of upstanding pins 130.The underside of base frame 101 is coated with a peelable adhesivebacking 145.

Spacer frame 102 defines an aperture 110 which can be divided into afirst portion 120 and a second portion 125. A transparent flexiblewindow 140 is secured to the spacer frame 102 over first portion 120 ofaperture 110. Spacer frame 102 further includes apertures 131 formedtherethrough frame 102 corresponding to pins 130 on the base frame 101.

Cover plate 103 defines the first portion 120 of aperture 110 andfurther includes apertures 132 formed therethrough corresponding to pins130 on the base frame 100. The cover plate 103 also includes atransparent semi-cylindrical housing 150 dimensioned and shaped to seatover a cylindrical Luer fitting positioned in the second portion 125 ofaperture 110. Housing 150 is preferably rigid for added protection andsecurement of the Luer fitting underneath. A rigid housing alsominimizes the risk of dislodging or displacing the IV holder or IVneedle by the patient's actions. The housing 150 may also include othercovers or members shaped to cover portions of an IV needle or fittings.

In use, the base frame 101 is adhesively secured to the patient's skinafter the insertion of the IV needle. Spacer frame 102 and cover plate103 are then mounted on base frame 101 by matching pins 130 withapertures 131 and 132. Ideally, the base frame 101 is positioned so thatthe IV needle is in the first portion 120 of aperture 110 and the Luerfitting is in second portion 125 of aperture 110 aperture 125 and underthe housing 150 of cover plate 103.

While base frame 101, spacer frame 102 and cover plate 103 are shown tobe generally coextensive with each other in FIG. 5, it should berecognized that this need not be the case. For example, the cover plate103 can be limited to the material between dashed lines 160 and 161.Moreover, the spacer frame 102 and cover plate 103 can be integratedinto a single unit.

Housing 150 is be preferably designed to be universally applied to andused with most if not all Luer fittings in the marketplace.Alternatively, housing 150 can be designed so that its interior has araised surface complementing a similar surface on a matching Luerfitting 170.

FIG. 6 shows a kit with an IV holder and an accompanying Luer fitting.The IV holder 200 comprises a base plate 201 which is adhesively securedto the patient's skin, the base plate forming an aperture 210 and havingupstanding pins 230 around its perimeter. The aperture 210 can bedivided into a first portion 215 and a second portion 220, shown by thedashed line 217. Cover plate 202 fits on top of base plate 201 and issecured by apertures 232 corresponding to upstanding pins 230. Coverplate 202 further has a window 240 positioned over the first portion 215of aperture 210 to cover the needle insertion site and a transparenthousing 250 positioned over the second portion 220 of aperture 210 forsecuring a Luer fitting 270. The outer surface of Luer fitting 270 isshown with a pattern of grooves complementing a pattern of grooves onthe inside of housing 250 such that when the housing 250 is positionedover Luer fitting 270, they are securely mated.

In lieu of grooves, the complementary surfaces of the interior ofhousing 250 and the outer surface of Luer fitting 270 can be designedusing ridges, tabs, or other uneven surfaces. In addition to providingan additional level of securement between the Luer fitting and the IVholder, such a design promotes the use of matching sizes of IV holdersand Luer fittings.

While the various descriptions of the present invention are describedabove, it should be understood that various features can be used singlyor in combination thereof. Therefore, this invention is not to belimited to the specific preferred embodiments depicted herein. Further,it should be understood that variations and modifications within thespirit and scope of the invention may occur to those skilled in the artto which the invention pertains. Accordingly, all expedientmodifications readily attainable by one versed in the art from thedisclosure set forth herein that are within the scope and spirit of thepresent invention are to be included as further embodiments of thepresent invention. The scope of the present invention is accordingly setforth in the appended claims.

What is claimed is:
 1. A holder for securing an intravenous needle, aLuer fitting, and an attached IV tube to a patient comprising: a baseframe with a top surface, a bottom surface, and a perimeter defining abase frame aperture, the base frame aperture having a circumferenceentirely enclosed by the perimeter of the base frame and forming apassage through the top and bottom surfaces of the base frame, whereinthe passage of the base frame aperture is divided into a first baseframe aperture portion and a second base frame aperture portion, thefirst base frame aperture portion being larger than the second baseframe aperture portion; at least a portion of the bottom surface of thebase frame having an adhesive adapted to secure the base frame to theskin; and a cover plate comprising a housing and a transparent flexiblecovering, the cover plate having a perimeter defining a cover plateaperture having a circumference entirely enclosed by the perimeter ofthe cover plate, wherein the perimeter of the cover plate is coextensivewith the perimeter of the base frame, and the cover plate aperture isdivided into a first cover plate aperture portion and a second coverplate aperture portion, the first cover plate aperture portion beinglarger than the second cover plate aperture portion, the housingcomprising a first material and extending over the second cover plateaperture portion, and the transparent flexible covering comprising asecond material and extending over the first cover plate apertureportion, wherein the first material is a different material than thesecond material such that the transparent flexible covering is moreflexible than the housing; wherein the cover plate is removably securedto the top surface of the base frame with the housing extending over thesecond base frame aperture portion and configured to engage against aLuer fitting positioned in the second cover plate aperture portion, andthe transparent flexible covering extending over the first base frameaperture portion, such that the transparent flexible covering can engageagainst the skin.
 2. The holder of claim 1, wherein the base framecomprises a pin extending from the top surface of the base frame, andthe cover plate comprises a pin aperture configured to engage the pin toremovably secure the cover plate and the base frame together.
 3. Theholder of claim 1, further comprising a spacer frame substantiallycoextensive with the base frame, the spacer frame being mountablebetween the top surface of the base frame and a bottom surface of thecover plate.
 4. The holder of claim 3, wherein the spacer framecomprises a perimeter defining a spacer frame aperture, and a secondtransparent flexible covering is secured to the spacer frame over aportion of the spacer frame aperture.
 5. The holder of claim 3, whereinthe base frame comprises a pin extending from the top surface of thebase frame, and the spacer frame and cover plate comprise a pin apertureconfigured to engage the pin to removably secure the base frame, spacerframe, and cover plate together.
 6. The holder of claim 1, wherein thehousing is semi-cylindrical.
 7. The holder of claim 1, wherein thehousing is substantially rigid.
 8. The holder of claim 1, wherein thehousing comprises an inner surface configured to engage against an outersurface of the Luer, the inner surface of the housing and the outersurface of the Luer fitting comprise interlocking grooves to restrictmovement between the housing and the Luer fitting.
 9. The holder ofclaim 1, wherein the housing comprises an inner surface configured toengage against an outer surface of the Luer, the inner surface of thehousing comprises a protrusion or a recess, and the Luer fittingcomprises the other of the protrusion or the recess to restrict movementbetween the housing and the Luer fitting.
 10. The holder of claim 1,wherein the transparent flexible covering comprises a bottom surfacecomprising an adhesive.
 11. The holder of claim 1, wherein the baseframe aperture is defined by the entire perimeter of the base frame.